6-(Chloromethyl)-2-methylpyrimidin-4(1H)-one, with the CAS number 35252-96-1, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains both nitrogen and carbon atoms. This compound features a chloromethyl group (-CH2Cl) at the 6-position and a methyl group (-CH3) at the 2-position of the pyrimidine ring, along with a carbonyl group (C=O) at the 4-position, contributing to its reactivity and potential applications in organic synthesis. The presence of the chloromethyl group makes it a useful intermediate in the synthesis of various pharmaceuticals and agrochemicals, as it can participate in nucleophilic substitution reactions. Additionally, the compound's structure suggests it may exhibit biological activity, although specific biological properties would require further investigation. Its solubility and stability can vary depending on the solvent and conditions, making it important to consider these factors in practical applications. Overall, this compound is of interest in medicinal chemistry and synthetic organic chemistry due to its functional groups and structural features.

6-(chloromethyl)-2-methylpyrimidin-4(1H)-one

35252-96-1: 6-(Chloromethyl)-2-methylpyrimidin-4(1H)-one, with the CAS number 35252-96-1, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains both nitrogen and carbon atoms. This compound features a chloromethyl group (-CH2Cl) at the 6-position and a methyl group (-CH3) at the 2-position of the pyrimidine ring, along with a carbonyl group (C=O) at the 4-position, contributing to its reactivity and potential applications in organic synthesis. The presence of the chloromethyl group makes it a useful intermediate in the synthesis of various pharmaceuticals and agrochemicals, as it can participate in nucleophilic substitution reactions. Additionally, the compound's structure suggests it may exhibit biological activity, although specific biological properties would require further investigation. Its solubility and stability can vary depending on the solvent and conditions, making it important to consider these factors in practical applications. Overall, this compound is of interest in medicinal chemistry and synthetic organic chemistry due to its functional groups and structural features.

CAS 35252-96-1

6-(chloromethyl)-2-methylpyrimidin-4(1H)-one

6-(Chloromethyl)-2-methylpyrimidin-4-ol

Ref: IN-DA00C8EI

6-(Chloromethyl)-2-methylpyrimidin-4-ol

Ref: 10-F239169